Article ID Journal Published Year Pages File Type
8509007 Bulletin of Faculty of Pharmacy, Cairo University 2017 5 Pages PDF
Abstract
Ximenia americana is used in African ethno-medicine for spasmodic bowel diseases with stem bark particularly used for ulcers. This study evaluated the toxicity-profile of methanol stem-bark extract. Extract doses were selected from estimated oral median lethal dose (LD50) of acute toxicity test. Ten male Wistar rats in 4-groups, weekly weighed and daily treated orally per body-weight for 28 days with normal-saline and extract-doses (250, 500, 1000 mg/kg) respectively were euthanized. Blood for biochemical and haematological analyses were collected into plain and anticoagulated (EDTA) sample-bottles respectively from each group. Vital-organs were isolated, weighed and fixed in buffered-formalin fixatives for histo-analyses. Mean ± standard-error of mean and statistical-significance at (p ≤ 0.05) of obtained-data were evaluated. The extract at up to 5000 mg/kg caused no mortality or behavioural toxic-signs and thus, oral LD50 was estimated to be greater than 5000 mg/kg. No changes in organ-sizes, body-weights or anatomy of brain, heart, liver and stomach occurred, but at 1000 mg/kg, kidney showed vascular-congestion with polymorphonuclear cells, lungs had consolidated areas of polymorphs infiltration, while spleen had distorted germinal-centres. Liver enzymes and urea levels were not altered significantly, but a dose dependent significant increase in total-protein only at 1000 mg/kg; and significant reduction in albumin level at 500 and 1000 mg/kg were observed. The observed dose-dependent reduction in creatinine was not significant. Total-calcium and chloride ion concentrations increased significantly only at 250 mg/kg. In conclusion, acute oral administration of methanol stem-bark extract of Ximenia americana was relatively non-toxic in mice, but minimal anatomical changes in kidney, lungs and spleen occurred when used for few weeks in rats.
Related Topics
Health Sciences Pharmacology, Toxicology and Pharmaceutical Science Drug Discovery
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